Local No. 8 IBEW Retirement Plan v. Vertex Pharmaceuticals Inc.

140 F. Supp. 3d 120, 2015 U.S. Dist. LEXIS 133063, 2015 WL 5749448
CourtDistrict Court, D. Massachusetts
DecidedSeptember 30, 2015
DocketCivil Action No. 14-12296-FDS
StatusPublished
Cited by6 cases

This text of 140 F. Supp. 3d 120 (Local No. 8 IBEW Retirement Plan v. Vertex Pharmaceuticals Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Massachusetts primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Local No. 8 IBEW Retirement Plan v. Vertex Pharmaceuticals Inc., 140 F. Supp. 3d 120, 2015 U.S. Dist. LEXIS 133063, 2015 WL 5749448 (D. Mass. 2015).

Opinion

MEMORANDUM AND ORDER ON DEFENDANTS’ MOTION TO DISMISS . (

SAYLOR, District Judge

This is a putative class action involving alleged violations ■ of the Securities Exchange Act of 1934 and Rule 10b-5. Local No. 8 IBEW Retirement Plan has brought suit, on behalf of a class of similarly situated -persons,- against Vertex Pharmaceuticals Inc. and various Vertex executives. Plaintiff contends that class members were harmed when they purchased Vertex’s common stock at prices that were artifi-[125]*125dally inflated by the company’s false and misleading statements about its products. Plaintiff also contends that a number of Vertex executives personally profited by selling millions of dollars of Vertex stock while the stock’s value was artificially inflated.

Defendants have filed a motion to dismiss pursuant to Fed. R, Civ. P. 12(b)(6) on the ground that the complaint fails to state a claim under the heightened pleading requirements for actions alleging securities fraud. It is essentially undisputed that Vertex made a false statement on May 7, 2012, when it released the interim results of a Phase II clinical study concerning a combination therapy for cystic fibrosis. For purposes of the moti'on to dismiss, Vertex also does not dispute that the false statement was material. The only issue is whether the complaint pleads sufficient facts to give rise to a “strong inference” of scienter, as required by law. For the reasons set forth below, defendants’ motion will be granted.

I. Background

Unless otherwise noted, all facts are stated as set forth in the complaint.1

A. Factual Background

■Vertex is a biotechnology company that researches, develops, and commercializes pharmaceuticals to treat a variety of illnesses. (Compl. ¶¶ 3, 20). The company’s products include treatments for hepatitis C, HIV, and cancer. (Id. ¶¶ 3, 20). At the relevant time, Vertex was based in Cambridge, Massachusetts, (Id. ¶¶ 12,20).

Joshua Boger, PhD., founded Vertex in 1989. (Id. ¶¶ 3, 13). He was formerly the Chief Executive Officer and Chairman of the Board; in 2012, he was serving as a Director. (Id. ¶ 13). Jeffrey Leiden, M.D., Ph.D., was the President and Chief Executive Officer of Vertex. (Id. ,¶ 14). Peter Mueller, Ph.D., was the Executive Vice President of Global Research & Development. (Id. ¶ 15). Elaine Ullian was the co-lead independent director. (Id. ¶ 17). From 2008 to April 2011, Paul Silva served as Vice President and Corporate Controller. (Id. ¶ 16). From December 2009 to June 2012, Nancy J. Wysenski was Chief Commercial Officer and Executive Vice President. (Id. ¶ 18).

One of Vertex’s products is the drug Kalydeco, which was approved by the Food and Drug Administration for use in treating- cystic fibrosis in early 2012. (Id. ¶¶ 4, 22).

Cystic fibrosis is a disease that causes the body to produce abnormal amounts of mucus in the lungs and the pancreas. (Id. ¶ 23). It typically results in life-threatening lung infections and digestion problems. (Id.). Approximately 30,000 people in the United States have cystic fibrosis. (Id.). Currently, there is no cure for the disease. (Id).

Cystic fibrosis is a genetic disease. (Id). It is caused by mutations that affect a particular protein, so that, among other things, the protein does not properly regulate the movement of chloride in and out of the lungs. (Id. ¶ 24). The majority of cases involve the “F508del” mutation. (Id). Approximately four percent of cases .involve the' “G551D” mutation. (Id. ¶¶ 22,24).

[126]*126In January 2012, Vertex received FDA approval for use of Kalydeco with patients who had the G551D mutation. (Id. ¶ 22). In early 2012, Vertex also began exploring the combination of Kalydeco with another medication, VX-809. (Id. ¶¶ 22,24).

Vertex began its Phase II trial of VX-809 and Kalydeco in combination by enrolling 108'patients for the study. (Id. ¶ 25). Patients were asked to cease their antibiotic treatments, as most cystic fibrosis patients cycle antibiotics and tend to deteriorate when off the antibiotics. (Id.). Varying dosages of VX-809 were given to patients for 28 days, followed by Kalydeco for 28 days. (Id.). The control group received placebo pills during the entire 56-day period. (Id.)

On May 7, 2012, Vertex announced in a press release that it had achieved significant “interim results” in the Phase II clinical study that combined VX-809 and Kaly-deco. (Id. ¶ 28; Sylvia Aff. Ex. A).2 The press release stated that “approximately 46 percent (17/37) [of patients] experienced an absolute improvement from baseline to Day 56 in lung function of 5 percentage points or more,” and that “approximately 30 percent (11/37) experienced an absolute improvement from baseline to Day 56 of 10 percentage points or more.” (Compl ¶ 28) (emphasis added). The press release also noted that in comparison, none of the patients treated with placebo achieved an improvement of five percentage points or more. (Id.). The press release included information about sweat chloride levels and stated that the “reductions were not statistically significant.” (See Sylvia Aff. Ex. A at 3).3

Vertex held a conference call with analysts on May 7. (Compl. 1Í 30). During the call, Mueller, the Chief Scientific Officer, remarked that he had “never seen anything like this” and called the results “really fantastic.” (Id. ¶ 30). Leiden, the Chief Executive Officer, remarked that Vertex’s hepatitis C drug and Kalydeco had provided significant cash flows to the company and indicated that it would “accelerate” its investment into the next stage. (Id. ¶ 31). Wysenski, the Chief Commercial Officer, said that the potential market for the treatment was 70,000 patients, which would amount to billions of dollars of potential sales. (Id.).4

At the end of the day on May 7, Vertex’s stock price, which had closed at $37.41 per [127]*127share on May 4, closed at $58.12 per share. (Id. ¶ 34). Trading volume that day was 40 times the average. (Id.). In the subsequent weeks, the company’s stock price climbed as high as $64.94. (Id. ¶ 35).

The complaint alleges that defendants “turned a blind eye” to the likelihood that the released results were “too good to be true.” (Id. ¶ 40). According to a- confidential witness (“CW2”) who was a Vertex senior director from 2004 to June 2012, the company had the results for two weeks prior to releasing them; the results “would have been sent” to defendant Wysenski and others, and a committee of executives “met to review the results to determine whether the information was material and warranted release.” (Id. ¶ 41) .5 Another witness (“CW1”), who worked at Vertex prior to 2012, states that some employees were highly skeptical of the results because there was a noted lack of sweat chloride improvement and the data announced on May 7, 2012 was just “too beautiful” and needed to be checked. (Id. ¶ 42).

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140 F. Supp. 3d 120, 2015 U.S. Dist. LEXIS 133063, 2015 WL 5749448, Counsel Stack Legal Research, https://law.counselstack.com/opinion/local-no-8-ibew-retirement-plan-v-vertex-pharmaceuticals-inc-mad-2015.